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NCT01971372 · ClinicalTrials.gov registry record

Post-Operative Pain Management With NSAIDS

A clinical trial of Urogynecologic Surgery, sponsored by University of Oklahoma.

Completed
Registry status
120
Enrollment target
1
Study location

NCT01971372: Completed study of Urogynecologic Surgery, sponsored by University of Oklahoma.

NCT01971372 is a study of Urogynecologic Surgery that has completed, run by University of Oklahoma. The registered enrollment target is 120 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01971372, a study of Urogynecologic Surgery, has completed, sponsored by University of Oklahoma.

COMPLETED
Registry status
120 participants
Enrollment target
1
Study location

Study Summary

Specific Aim 1: To identify differences in pain perception and satisfaction with pain control in women undergoing urogynecologic surgery receiving nonsteroidal anti-inflammatory (NSAIDS) postoperatively by oral ibuprofen, intravenous ibuprofen, or intravenous ketorolac. Specific Aim 2: To compare the differences in narcotic usage and medication side effects.

Primary Outcome

Three visual analog scores (VAS) will be obtained from the patient before noon on the first day after surgery. One scale to assess pain at rest, one scale to assess pain with ambulation, and one scale to assess satisfaction with pain control.

Conditions Studied

Study Locations (1)

Oklahoma

  • University of Oklahoma Health Sciences Center - Oklahoma City

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2013-09
Est. Completion 2015-11
University of Oklahoma

358 total trials

What the finished NCT01971372 record still lists

NCT01971372 is an observational study that tracks outcomes without assigning an intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap.

The record links to 1 condition, with Urogynecologic Surgery appearing as the primary indexed condition, and to 0 interventions.

NCT01971372 reports a single indexed study location in Oklahoma.

Frequently Asked Questions

What is clinical trial NCT01971372 about?

NCT01971372 is a clinical study titled "Post-Operative Pain Management With NSAIDS". Specific Aim 1: To identify differences in pain perception and satisfaction with pain control in women undergoing urogynecologic surgery receiving nonsteroidal anti-inflammatory (NSAIDS) postoperatively by oral ibuprofen, intravenous ibuprofen, or intravenous ketorolac. Specific Aim 2: To compare th...

What is the current status of trial NCT01971372?

This trial is currently completed. The enrollment target is 120 participants. The study started on 2013-09. Estimated completion is 2015-11.

What conditions does trial NCT01971372 study?

This clinical trial studies the following conditions: Urogynecologic Surgery.

Who is sponsoring clinical trial NCT01971372?

This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01971372 being conducted?

This trial has 1 study location across Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT01971372, the US trial registry maintained by the National Library of Medicine. NCT01971372 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.